메뉴 건너뛰기




Volumn 76, Issue 23, 2011, Pages 9555-9567

Reactivity and synthesis inspired by the Zincke ring-opening of pyridines

Author keywords

[No Author keywords available]

Indexed keywords

CASCADE REACTIONS; CONCISE SYNTHESIS; CYCLOADDITION REACTION; DEAROMATIZATION; EFFICIENT PROCESS; FORMAL SYNTHESIS; HETEROCYCLE SYNTHESIS; INDOLE ALKALOIDS; NATURAL PRODUCTS; PYRIDINIUM SALTS; PYRROLINES; RING OPENING; UNSATURATED AMIDES;

EID: 82255182364     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo201625e     Document Type: Review
Times cited : (70)

References (81)
  • 2
    • 82255184086 scopus 로고    scopus 로고
    • Furans
    • In; Li, J. J. John Wiley & Sons: Hoboken
    • Shea, K. M. Furans. In Name Reactions in Heterocyclic Chemistry; Li, J. J., Ed.; John Wiley & Sons: Hoboken, 2005; pp 168-181.
    • (2005) Name Reactions in Heterocyclic Chemistry , pp. 168-181
    • Shea, K.M.1
  • 3
    • 27844586676 scopus 로고    scopus 로고
    • Furans: Reactions and Synthesis
    • 4 th ed. Blackwell Publishing: Oxford
    • Joule, J. A.; Mills, K. Furans: Reactions and Synthesis. Heterocyclic Chemistry, 4 th ed.; Blackwell Publishing: Oxford, 2000; pp 308-309.
    • (2000) Heterocyclic Chemistry , pp. 308-309
    • Joule, J.A.1    Mills, K.2
  • 4
    • 14744305251 scopus 로고    scopus 로고
    • For a comprehensive review of furan synthesis methods, including the Paal - Knorr method, see
    • For a comprehensive review of furan synthesis methods, including the Paal - Knorr method, see: König, B. Sci. Synth. 2002, 9, 183-285
    • (2002) Sci. Synth. , vol.9 , pp. 183-285
    • König, B.1
  • 17
    • 77953490105 scopus 로고    scopus 로고
    • For another interesting connection between furans and 5-amino-2,4-pentadienals, which are the subject of this Perspective, see
    • For another interesting connection between furans and 5-amino-2,4-pentadienals, which are the subject of this Perspective, see: Ouairy, C.; Michel, P.; Delpech, B.; Crich, D.; Marazano, C. J. Org. Chem. 2010, 75, 4311-4314
    • (2010) J. Org. Chem. , vol.75 , pp. 4311-4314
    • Ouairy, C.1    Michel, P.2    Delpech, B.3    Crich, D.4    Marazano, C.5
  • 22
    • 37049169153 scopus 로고
    • Birch pioneered the combined alkali metal reduction/hydrolysis/aldol cyclization approach to cyclohexenones
    • Birch pioneered the combined alkali metal reduction/hydrolysis/aldol cyclization approach to cyclohexenones: Birch, A. J. J. Chem. Soc. 1947, 1270
    • (1947) J. Chem. Soc. , pp. 1270
    • Birch, A.J.1
  • 69
    • 0032725566 scopus 로고    scopus 로고
    • Zincke aldehydes are known to be recalcitrant dienes in intermolecular cycloadditions: and references therein
    • Zincke aldehydes are known to be recalcitrant dienes in intermolecular cycloadditions: Baldwin, J. E.; Claridge, T. D. W.; Culshaw, A. J.; Heupel, F. A.; Lee, V.; Spring, D. R.; Whitehead, R. C. Chem. - Eur. J. 1999, 5, 3154-3161 and references therein
    • (1999) Chem. - Eur. J. , vol.5 , pp. 3154-3161
    • Baldwin, J.E.1    Claridge, T.D.W.2    Culshaw, A.J.3    Heupel, F.A.4    Lee, V.5    Spring, D.R.6    Whitehead, R.C.7
  • 72
    • 84982062020 scopus 로고
    • For the most closely related rearrangement that we have found in the literature, see
    • For the most closely related rearrangement that we have found in the literature, see: Roedig, A.; Göpfert, H. Chem. Ber. 1981, 114, 3625-3633
    • (1981) Chem. Ber. , vol.114 , pp. 3625-3633
    • Roedig, A.1    Göpfert, H.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.